To author and gain approval of scientific and regulatory submission documents that comply with global regulatory standards. To maintain key business relationships with appropriate cross-functional product team members.

Bachelors degree, Diploma in Pharmacy. One Year experience in related field. funded project titled Structuring district level services for management of headache disorders;

Pharmacist degree from a recognized institution, registration with Gujarat Pharmacist Council is required.

Master, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement

Masters in Natural or Agricultural or Pharmaceutical Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement; Establishing an IP search resource center at NCL

Conduct high-quality research in molecular biology and industrial biotechnology. Design and execute experiments, analyze data, and interpret results. Collaborate with a multidisciplinary team of scientists and researchers.

M.Sc, B.Tech in Biotechnology, Bioinformatics, Biochemistry, Agricultural Biotechnology, Molecular Biology, Life Sciences, Botany. Knowledge of molecular biology techniques, Metabolite analysis. 

Monitor Global and Europe and Canadian markets for new product opportunities in both branded and Generic space In depth understanding of new product selection processes including portfolio management Primary responsibilities for executing out-licensing activities for the companies approved and In-development projects including financial modelling

Macleods is one of the fastest growing pharmaceutical company, having strong presence in various therapeutics segments. Ranked amongst the top 10 companies.

01 to 05 with relevant functional experience in injectable manufacturing, Aseptic area operations, Packing, Visual inspection, QMS activities

Quality Management System oversight and implementation, Validation processes for production systems, In-Process Quality Assurance for General Injectable and Oral Solid Dosage forms.

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control.

Demonstrated experience in pharmaceutical, life sciences preferred or healthcare in the data areas of patient or HCP, HCO data, sales and marketing data, financial, or product data.

Author Safety Data Sheets for multiple geographies across the globe as per applicable hazard communication regulations. Derive hazard classifications for substances and mixtures using various classification regulations including but not limited to GHS, CLP, and OSHA Hazard Communication Standard.

Eli Lilly and Company announced the U.S. Food and Drug Administration approved Zepbound tirzepatide as the first and only prescription medicine for adults with moderate-to-severe obstructive sleep apnea OSA and obesity.

D.Pharm from Government an approved Indian Medicine Institution and affiliated with the Tamilnadu Dr. M.G.R. Medical University

Project coordination, data collection, field level supervision of data collection, qualitative interviewing, development of IEC materials and networking with local communities and health officials. Patient recruitment, follow-up, communication and interaction.

It caters to the field of drug testing and analysis for human samples with its state of art facility including GC, MS, GC-MS, MS, LC-MS, MS, HPLC, GC, C, IRMS, ELISA, protein separation and identification tools towards the goal of making sports free from doping. NDTL offers opportunity of training facility for deserving students in both summer and winter January-June sessions. The training will be for a period of 6 months for the students from different universities, institutions in areas of drug, metabolite testing and analysis